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Diagnostics (Basel, Switzerland)|September 25, 2019
Analytical Evaluation of an NGS Testing Method for Routine Molecular Diagnostics on Melanoma Formalin-Fixed, Paraffin-Embedded Tumor-Derived DNAIrene Mancini, Lisa Simi, Francesca Salvianti, et al.
Diagnostics (Basel, Switzerland)|September 25, 2019
Coronary Artery Microcalcification: Imaging and Clinical ImplicationsFederico Vancheri, Giovanni Longo, Sergio Vancheri, et al.
Diagnostics (Basel, Switzerland)|August 17, 2019
Development of a Highly Sensitive Technique for Capturing Renal Cell Cancer Circulating Tumor CellsMichio Naoe, Chiho Kusaka, Mika Ohta, et al.
Diagnostics (Basel, Switzerland)|August 21, 2019
Differential Expression Profiles of the Transcriptome and miRNA Interactome in Synovial Fibroblasts of Rheumatoid Arthritis Revealed by Next Generation SequencingChia-Chun Tseng, Ling-Yu Wu, Wen-Chan Tsai, et al.
Diagnostics (Basel, Switzerland)|October 5, 2019
Serum Anti-Müllerian Hormone in the Diagnosis of Polycystic Ovary Syndrome in Association with Clinical SymptomsNada Ahmed, Asma A Batarfi, Osama S Bajouh, et al.
Diagnostics (Basel, Switzerland)|March 3, 2019
Disseminated Bartonella henselae Infection Visualized by [18F]FDG-PET/CT and MRIMarie Norredam, Andreas Knudsen, Carsten Thomsen, et al.
Diagnostics (Basel, Switzerland)|February 21, 2019
Introduction to Special Issue on "Electromagnetic Technologies for Medical Diagnostics: Fundamental Issues, Clinical Applications and Perspectives"Panagiotis Kosmas, Lorenzo Crocco
Diagnostics (Basel, Switzerland)|February 9, 2021
Impact of Lymphovascular Invasion on Prognosis in the Patients with Bladder Cancer-Comparison of Transurethral Resection and Radical CystectomyKei Yoneda, Naoto Kamiya, Takanobu Utsumi, et al.
Diagnostics (Basel, Switzerland)|February 11, 2021
Differences in Clinical Characteristics and Chest Images between Coronavirus Disease 2019 and Influenza-Associated PneumoniaSi-Ho Kim, Yu Mi Wi, Sujin Lim, et al.
Diagnostics (Basel, Switzerland)|February 11, 2021
NGS Gene Panel Analysis Revealed Novel Mutations in Patients with Rare Congenital Diarrheal DisordersMaria Valeria Esposito, Marika Comegna, Gustavo Cernera, et al.
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